ENST00000258439.8:c.272T=
MANE Select
|
ENSP00000258439.3:p.Leu91=
|
|
ENST00000258439.7:c.272T=
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ENSP00000258439.2:p.Leu91=
|
|
ENST00000432959.1:c.272T=
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ENSP00000416660.1:p.Leu91=
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|
ENST00000435268.1:c.20T=
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ENSP00000411810.1:p.Leu7=
|
|
NM_001193304.2:c.272T=
|
NP_001180233.1:p.Leu91=
|
|
NM_017849.3:c.272T= , LRG_528t1:c.272T=
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NP_060319.1:p.Leu91=
|
|
XM_017004450.1:c.-647T=
|
XP_016859939.1:n.-647T=
|
|
XM_017004452.1:c.20T=
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XP_016859941.1:p.Leu7=
|
|
NM_001193304.3:c.272T=
|
NP_001180233.1:p.Leu91=
|
|
NM_017849.4:c.272T=
MANE Select
|
NP_060319.1:p.Leu91=
|
|